Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED NA

Effects of Pneumatic Vitreolysis on Macular Hole

NCT03677869 · View on ClinicalTrials.gov ↗

Study Summary

Eyes with vitreomacular traction (VMT) and full-thickness macular holes (MH) will be enrolled into a non-randomized cohort treated with pneumatic vitreolysis (PVL) to determine the proportion with VMT release and MH closure and to assess factors associated with success.

Interventions

  • DEVICE Intraocular gas (C3F8)

Study Locations (20)

Florida

  • National Ophthalmic Research Institute — Fort Myers
  • University of Florida College of Med., Dept of Ophthalmology, Jacksonville Hlth Sci Ctr — Jacksonville
  • Florida Retina Consultants — Lakeland
  • Florida Retina Institute — Orlando
  • Southeast Eye Institute, PA dba Eye Associates of Pinellas — Pinellas Park
  • Retina Associates of Sarasota — Sarasota
  • Sarasota Retina Institute — Sarasota

California

  • Retinal Diagnostic Center — Campbell
  • Atlantis Eye Care — Huntington Beach
  • Northern California Retina Vitreous Associates — Mountain View
  • East Bay Retina Consultants, Inc. — Oakland
  • Southern California Desert Retina Consultants, MC — Palm Desert

Illinois

  • Gailey Eye Clinic — Bloomington
  • University of Illinois at Chicago Medical Center — Chicago
  • Illinois Retina Associates, SC — Oak Park
  • Carle Foundation Hospital — Urbana

Georgia

  • Southeast Retina Center, PC — Augusta
  • Thomas Eye Group — Sandy Springs

Indiana

  • Raj K. Maturi, MD, PC — Indianapolis

Iowa

  • Wolfe Eye Clinic — West Des Moines

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2018-11-14
Est. Completion 2020-07-22
Phase NA

Sponsor

Jaeb Center for Health Research

134 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03677869

The ClinicalTrials.gov registry entry for NCT03677869 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Jaeb Center for Health Research, which has 134 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Vitreomacular Traction (VMT) appearing as the primary indexed condition, and to 1 intervention — of which Intraocular gas (C3F8) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03677869 reports 20 study locations spanning 6 distinct geographic areas — top geographies include Florida, California, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03677869 about?

NCT03677869 is a clinical study titled "Effects of Pneumatic Vitreolysis on Macular Hole". Eyes with vitreomacular traction (VMT) and full-thickness macular holes (MH) will be enrolled into a non-randomized cohort treated with pneumatic vitreolysis (PVL) to determine the proportion with VMT release and MH closure and to assess factors associated with success.

What is the current status of trial NCT03677869?

This trial is currently completed. It is a NA study. The enrollment target is 36 participants. The study started on 2018-11-14. Estimated completion is 2020-07-22.

What conditions does trial NCT03677869 study?

This clinical trial studies the following conditions: Vitreomacular Traction (VMT), Full-thickness Macular Holes (MH). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03677869?

The interventions under investigation include: Intraocular gas (C3F8) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03677869?

This trial is sponsored by Jaeb Center for Health Research, which has 134 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03677869 being conducted?

This trial has 20 study locations across California, Florida, Georgia, Illinois, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial